Year |
Citation |
Score |
2018 |
Klosowski DW, Hethcox JC, Paull DH, Fang C, Donald JR, Shugrue CR, Pansick AD, Martin SF. Enantioselective Halolactonization Reactions using BINOL-derived Bifunctional Catalysts: Methodology, Diversification, and Applications. The Journal of Organic Chemistry. PMID 29717607 DOI: 10.1021/Acs.Joc.8B00490 |
0.633 |
|
2013 |
Shanahan CS, Fang C, Paull DH, Martin SF. Asymmetric Formal Total Synthesis of the Stemofoline Alkaloids: The Evolution, Development and Application of a Catalytic Dipolar Cycloaddition Cascade. Tetrahedron. 69: 7592-7607. PMID 24072939 DOI: 10.1016/J.Tet.2013.03.104 |
0.469 |
|
2013 |
Fang C, Paull DH, Hethcox JC, Shugrue CR, Martin SF. Enantioselective iodolactonization of disubstituted olefinic acids using a bifunctional catalyst. Organic Letters. 15: 972. PMID 23356976 DOI: 10.1021/ol400125b |
0.445 |
|
2012 |
Fang C, Paull DH, Hethcox JC, Shugrue CR, Martin SF. Enantioselective iodolactonization of disubstituted olefinic acids using a bifunctional catalyst. Organic Letters. 14: 6290-3. PMID 23199100 DOI: 10.1021/Ol3030555 |
0.62 |
|
2012 |
Fang C, Shanahan CS, Paull DH, Martin SF. Enantioselective formal total syntheses of didehydrostemofoline and isodidehydrostemofoline through a catalytic dipolar cycloaddition cascade. Angewandte Chemie (International Ed. in English). 51: 10596-9. PMID 22987285 DOI: 10.1002/Anie.201205274 |
0.461 |
|
2012 |
Paull DH, Fang C, Donald JR, Pansick AD, Martin SF. Bifunctional catalyst promotes highly enantioselective bromolactonizations to generate stereogenic C-Br bonds. Journal of the American Chemical Society. 134: 11128-31. PMID 22726214 DOI: 10.1021/Ja305117M |
0.6 |
|
2011 |
Erb J, Paull DH, Dudding T, Belding L, Lectka T. From bifunctional to trifunctional (tricomponent nucleophile-transition metal-lewis acid) catalysis: the catalytic, enantioselective α-fluorination of acid chlorides. Journal of the American Chemical Society. 133: 7536-46. PMID 21513338 DOI: 10.1021/Ja2014345 |
0.852 |
|
2009 |
Paull DH, Weatherwax A, Lectka T. Catalytic, asymmetric reactions of ketenes and ketene enolates. Tetrahedron. 65: 3771-6803. PMID 21494417 DOI: 10.1016/J.Tet.2009.05.079 |
0.784 |
|
2009 |
Abraham CJ, Paull DH, Dogo-Isonagie C, Lectka T. Diastereoselective Synthesis of trans-beta-Lactams Using a Simple Multifunctional Catalyst. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 10: 1651-1654. PMID 20442797 DOI: 10.1055/S-0029-1217348 |
0.79 |
|
2009 |
Lectka T, Paull D, Scerba M, Alden-Danforth E, Widger L. α-Fluorination of Acid Chlorides Synfacts. 2009: 0291-0291. DOI: 10.1055/S-0028-1087785 |
0.772 |
|
2009 |
Abraham CJ, Paull DH, Dogo-Isonagie C, Lectka T. ChemInform Abstract: Diastereoselective Synthesis of trans-β-Lactams Using a Simple Multifunctional Catalyst. Cheminform. 40. DOI: 10.1002/chin.200944111 |
0.78 |
|
2009 |
Paull DH, Scerba MT, Alden-Danforth E, Widger LR, Lectka T. ChemInform Abstract: Catalytic, Asymmetric α-Fluorination of Acid Chlorides: Dual Metal-Ketene Enolate Activation. Cheminform. 40. DOI: 10.1002/chin.200920034 |
0.792 |
|
2008 |
Abraham CJ, Paull DH, Bekele T, Scerba MT, Dudding T, Lectka T. A surprising mechanistic "switch" in Lewis acid activation: a bifunctional, asymmetric approach to alpha-hydroxy acid derivatives. Journal of the American Chemical Society. 130: 17085-94. PMID 19053448 DOI: 10.1021/Ja806818A |
0.82 |
|
2008 |
Paull DH, Scerba MT, Alden-Danforth E, Widger LR, Lectka T. Catalytic, asymmetric alpha-fluorination of acid chlorides: dual metal-ketene enolate activation. Journal of the American Chemical Society. 130: 17260-1. PMID 19049284 DOI: 10.1021/Ja807792C |
0.79 |
|
2008 |
Paull DH, Abraham CJ, Scerba MT, Alden-Danforth E, Lectka T. Bifunctional asymmetric catalysis: cooperative Lewis acid/base systems. Accounts of Chemical Research. 41: 655-63. PMID 18402470 DOI: 10.1021/Ar700261A |
0.78 |
|
2007 |
Paull DH, Alden-Danforth E, Wolfer J, Dogo-Isonagie C, Abraham CJ, Lectka T. An Asymmetric, bifunctional catalytic approach to non-natural alpha-amino acid derivatives. The Journal of Organic Chemistry. 72: 5380-2. PMID 17555354 DOI: 10.1021/Jo070472X |
0.775 |
|
2007 |
Paull DH, Wolfer J, Grebinski JW, Weatherwax A, Lectka T. Catalytic, asymmetric inverse electron demand hetero diels-alder reactions of o-benzoquinone derivatives and ketene enolates Chimia. 61: 240-246. DOI: 10.2533/Chimia.2007.240 |
0.825 |
|
2007 |
Lectka T, Abraham C, Paull D, Scerba M, Grebinski J. Bifunctional Inverse Electron Demand Hetero-Diels-Alder Reactions Synfacts. 2007: 0072-0072. DOI: 10.1055/S-2006-955718 |
0.767 |
|
2007 |
Dogo-Isonagie C, Bekele T, France S, Wolfer J, Weatherwax A, Taggi AE, Paull DH, Dudding T, Lectka T. A mechanistic study on the catalytic, asymmetric α-bromination of acid chlorides European Journal of Organic Chemistry. 1091-1100. DOI: 10.1002/Ejoc.200600819 |
0.766 |
|
2006 |
Abraham CJ, Paull DH, Scerba MT, Grebinski JW, Lectka T. Catalytic, enantioselective bifunctional inverse electron demand hetero-Diels-Alder reactions of ketene enolates and o-benzoquinone diimides. Journal of the American Chemical Society. 128: 13370-1. PMID 17031945 DOI: 10.1021/Ja065754D |
0.822 |
|
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